- IQVIA (Phoenix, AZ)
- …enrollment. The CTE works in partnership with CRAs and other field-based medical teams for optimal trial execution, developing tailored recruitment plans. ... require direct interaction with patients to offer education on trial , disease, and/or device /medication * May partner...organization equipment safely and in a good state of repair * Maintains up-to-date technical knowledge of specialty and… more
- IQVIA (Atlanta, GA)
- … * Some roles require direct interaction with patients to offer education on trial , disease, and/or device /medication * May partner with referral networks to ... Job Overview CTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a… more
- Edwards Lifesciences (Columbus, OH)
- …Degree in related field or equivalent + 5 years of medical device /sponsor/CRO/Pharma clinical field monitoring experience, quality assurance/control and ... As the Senior Clinical Research Monitor, you will ensure trial patients' safety by assuring trials are...regulatory compliance + Experience working in a medical device or regulated industry + Experience… more
- Edwards Lifesciences (Columbus, OH)
- …Degree in related field or equivalent + 5 years of medical device /sponsor/CRO/Pharma clinical field monitoring experience, quality assurance/control and ... As the Senior Clinical Research Monitor, you will ensure trial patients' safety by assuring trials are...regulatory compliance + Experience working in a medical device or regulated industry + Experience… more
- Edwards Lifesciences (Sacramento, CA)
- …in related field + 10 years' experience of industry medical device /sponsor/pharmaceutical/CRO, work experience in clinical trial management **OR** + Masters ... of Clinical Project Management, you will manage complex clinical trials activities and ensure all applicable regulatory requirements are...Degree with 8 years of industry medical device /sponsor/pharmaceutical/CRO clinical trial management… more
- Edwards Lifesciences (Columbus, OH)
- …assurance/control and regulatory compliance or field monitoring + Experience working in a medical device or regulated industry + Experience with electronic data ... Research Monitor on the Aortic team, you will ensure trial patients' safety by assuring trials are...Business Unit area of expertise + Substantial understanding of medical device regulatory requirements and documents, … more
- Edwards Lifesciences (St. Paul, MN)
- …**What else we look for (Preferred):** + Experience working in the medical device industry strongly preferred **Key Knowledge:** + Expert understanding ... in the Surgical Structural Heart Valve business unit to support various global medical and clinical activities. This is a fast-paced, dynamic team working on… more
- Edwards Lifesciences (San Diego, CA)
- …look for (Preferred):** + Experience as a biostatistician working in the medical device setting preferred + Extensive understanding in statistical methodologies ... understanding of regulatory guidelines (eg, GCP, ICH, FDA, ISO) relevant to the Medical Device research setting + Excellent written and verbal communication… more
- Edwards Lifesciences (Detroit, MI)
- …(RT), Operating Room Technician (ORT), or Cardiovascular Technician (RCIS) or related medical device , clinical, or Certification in RDCS (Registered Diagnostic ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
- Medtronic (Baltimore, MD)
- …M&T Structural Heart Business is one of the fastest growing businesses in the medical device industry and expanding rapidly to serve patients globally. The ... cardiac procedures + Clinical Research experience in structural heart or other medical devices + Experience coordinating multi-center cardiology trials +… more
- HCA Healthcare (Nashville, TN)
- …subject research. Job Responsibilities: + Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible ... data capture systems. + Generates and tracks drug shipments, device shipments, and supplies as needed. + Ensures timely...Director and Regional Site Manager of all study specific medical issues for guidance. + Assists sponsor and US… more
- Medtronic (Ocala, FL)
- …surgery, Surgical Aortic Valve Replacement (SAVR) experience preferred + Strong, proven medical device sales track record with documented growth and achievements ... **Bring your sales talents to a leader in medical technology and healthcare solutions.** **Rooted in our...with Medtronic guidance + Provide technical leadership for TAVR device procedures. Educate implanting teams on proper indications for… more
- Edwards Lifesciences (Irvine, CA)
- …biology or life Sciences field, with 5 Years experience Class II and III medical device technologies and/or clinical studies background Required **What else we ... assessments and/or clinical evaluation reports + Consult with field trial managers to gather field device performance...management skills + Full knowledge of US and international medical device regulations, of Good Laboratory Practice… more
- Indian Health Service (Pine Ridge, SD)
- …Specialist or designee. Responsibilities Assists with evaluation, installation, service and repair of highly complex medical equipment and systems. Communicate ... cost of repairs, updates/upgrades, modifications and other services performed on the device . Test/classifies medical equipment in current use and determines… more
- Edwards Lifesciences (Irvine, CA)
- …field, 3 years experience previous related experience in Class II and III medical device technologies and/or clinical studies background Required **What else we ... knowledge and understanding of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical studies +… more
- Catalent Pharma Solutions (Chelsea, MA)
- …and experience is required. + Experience in a cGMP biopharmaceutical, pharmaceutical, medical device , food, or other FDA regulated industry is preferred. ... lives. The **Equipment Maintenance Technician** is responsible for the service and repair of production and ancillary equipment at our facility. This position will… more
- University of Colorado (Boulder, CO)
- …management of department devices using tools such as the Jamf mobile device management platform and Microsoft Endpoint Configuration Manager (MECM). This position ... working alongside teammates in a collaborative environment to diagnose, troubleshoot, repair , and maintain university owned computer equipment, mobile devices, and… more
- Edwards Lifesciences (Tallahassee, FL)
- …regulatory guidelines (eg, GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/ Medical Device research setting + Excellent problem-solving, organizational, ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
- Medtronic (Boston, MA)
- …robotics teams as your career progresses. Careers that Change Lives Our space, the medical device and healthcare industry, is rapidly changing. It always has ... annually + Ranked in the top 10 (https://www.proclinical.com/blogs/2019-11/glassdoors%20top%2010%20medical%20device%20companies%20to%20work%20for) best medical device companies to work for A… more
- Edwards Lifesciences (Irvine, CA)
- …organizational, analytical and critical thinking skills . Experience working in clinical trials within a pharmaceutical/ medical device industry . Good ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more